Sun Chun-Yi, To Wai-Pong, Wang Xin-Long, Chan Kaai-Tung, Su Zhong-Min, Che Chi-Ming
State Key Laboratory of Synthetic Chemistry , Institute of Molecular Functional Materials , HKU-CAS Joint Laboratory on New Materials , Department of Chemistry , The University of Hong Kong , Pokfulam Road , Hong Kong , China . Email:
Institute of Functional Materials Chemistry , Northeast Normal University , Changchun , Jilin 130024 , China.
Chem Sci. 2015 Dec 1;6(12):7105-7111. doi: 10.1039/c5sc02216a. Epub 2015 Sep 21.
The encapsulation of luminescent gold(iii) complexes by metal-organic frameworks (MOFs) lays the groundwork for new phosphorescent materials with activities that are not readily achieved by the host MOF materials or gold(iii) complexes alone. In this work, strong phosphorescence with lifetimes of up to ∼50 μs in open air at room temperature has been achieved by incorporation of cationic cyclometalated gold(iii) complexes into MOFs with anionic frameworks to form Au@MOFs. The Au@MOFs display solid state two-photon-induced phosphorescence. Photo-reduction of methyl viologen to the reduced radical was achieved inside Au@MOFs and in the presence of EtN upon excitation at > 370 nm under ambient conditions. These Au@MOFs comprise a class of reusable and size-selective heterogeneous photo-catalysts for the aerobic oxidation of secondary amines to imines as well as five other reactions, including oxidative C-H functionalization under aerobic conditions.
金属有机框架(MOF)对发光金(III)配合物的封装为新型磷光材料奠定了基础,这类材料具有单独的主体MOF材料或金(III)配合物难以实现的活性。在这项工作中,通过将阳离子环金属化金(III)配合物引入具有阴离子框架的MOF中形成Au@MOF,在室温下的空气中实现了寿命长达约50 μs的强磷光。Au@MOF表现出固态双光子诱导磷光。在环境条件下,当在大于370 nm的波长激发时,在Au@MOF内部以及存在EtN的情况下,甲基紫精被光还原为还原自由基。这些Au@MOF构成了一类可重复使用且具有尺寸选择性的多相光催化剂,可用于将仲胺需氧氧化为亚胺以及其他五个反应,包括在需氧条件下的氧化C-H官能化反应。